HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,5-Dimethyl-1H-pyrazole-1-carboxamidine mononitrate → HCID 178512768, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,5-Dimethyl-1H-pyrazole-1-carboxamidine mononitrate | HCID 198186 | — |
| Reactant | 4-(aminomethyl)-2-iodoaniline | HCID 10354623 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178512768 | HCID 178512768 | — |
Reaction Steps
An ethanol (5 ml) solution of 3-iodo-4-aminobenzylamine (0.220 g, 0.887 mmol) and 3,5-dimethylpyrazole-1-carboxamidine nitrate (0.179 g, 0.087 mmol) was heated at reflux temperature for 3 hr. under argon. The solvent was evaporated in vacuo and the residue washed with ether and dichloromethane to remove 3,5-dimethylpyrazole and unreacted amine. The crude product was recrystallized from methanol/ether to give fine, pale-yellow needles (0.163 g, 72.5%), mp 135°-137° C.; PMR (DMSO-d6) γ6.62-7.66 (m, 9H), 4.1 (s, 2H); IR (Nujol) 1660, 1620 cm-1 (C=N); Anal. Calcd. for C18H11IN4. HNO3.0.5H2O): C, 27.20; H, 3.42, N, 19.08. Found C, 26.70; H, 3.33; N, 19.08.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04622217 |
| Source dataset | uspto-grants-1986_11 |
| ORD ID | ord-bd933e877c054d4b977bf8030efeafea |
| Source note | uspto-grants-1986_11 |